Реакция #1552019

ord-9e95a0e347ad4af396770b69ab968504

Уравнение реакции

CCC(C)=O
methyl ethyl ketone
Oc1ccc(-c2ccccc2)cc1
4-hydroxybiphenyl
OCCCCCCBr
6-bromo-1-hexanol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
OCCCCCCOc1ccc(-c2ccccc2)cc1
6-(4-phenylphenoxy)hexane-1-ol
Выход 75.8%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThis solution was refluxed for 24 hours
  2. 2
    Промывкаrinsed with water three times
  3. 3
    ДругоеThe organic phase was then separated
  4. 4
    Сушкаdried over magnesium sulfate
  5. 5
    workup.DISTILLATIONthe solvent was distilled off
  6. 6
    workup.DISSOLUTIONThe residue was dissolved in toluene
  7. 7
    Другоеpurified by recrystallization

Методика

To 80 mL of methyl ethyl ketone, 9.05 g (50 mmol) of 4-hydroxybiphenyl, 10.20 g (60 mmol) of 6-bromo-1-hexanol, and 20.7 g (150 mmol) of potassium carbonate were added. This solution was refluxed for 24 hours and then cooled to room temperature. This solution was diluted with 200 mL of methylene chloride and rinsed with water three times. The organic phase was then separated and dried over magnesium sulfate, and the solvent was distilled off. The residue was dissolved in toluene and purified by recrystallization to provide 10.25 g of 6-(4-phenylphenoxy)hexane-1-ol.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08998400B2uspto-grants-2015_04